Seregin Vladimir V, Coffer Jeffery L
Department of Chemistry, Texas Christian University, TCU Box 298860, Fort Worth, 76129, USA.
Biomaterials. 2006 Sep;27(27):4745-54. doi: 10.1016/j.biomaterials.2006.04.031. Epub 2006 Jun 5.
The incorporation of CaSi(2) grains within a polycaprolactone (PCL) framework results in bioactive and biodegradable scaffolds which may be used in bone tissue regeneration. Porous PCL scaffolds were prepared via a combination of salt-leaching and microemulsion methods. To provide markedly different structural environments for the inorganic phase, calcium disilicide powder was either added to a mixed-composition porogen during a given scaffold preparation, or alternatively added to pre-formed scaffolds. Selective fluorescent labeling, scanning electron microscopy (SEM), and energy dispersive X-ray (EDX) analysis were employed to assess scaffold calcification in vitro. The process of CaSi(2)/PCL scaffold calcification under zero bias, during which calcium phosphate growth is significantly dependent on the structural degradation of CaSi(2) grains, has a similar mechanism as the calcium phosphate growth on bioactive glasses/ceramics. The biomineralization of these scaffolds is initiated solely by the silicide phase and can be accelerated by the degradation of the polymer matrix.
将CaSi₂颗粒掺入聚己内酯(PCL)框架中可形成生物活性和可生物降解的支架,可用于骨组织再生。通过盐析和微乳液方法的组合制备了多孔PCL支架。为了给无机相提供明显不同的结构环境,在给定的支架制备过程中,将二硅化钙粉末添加到混合成分的致孔剂中,或者添加到预先形成的支架中。采用选择性荧光标记、扫描电子显微镜(SEM)和能量色散X射线(EDX)分析来评估支架在体外的钙化情况。CaSi₂/PCL支架在零偏压下的钙化过程中,磷酸钙的生长显著依赖于CaSi₂颗粒的结构降解,其机制与生物活性玻璃/陶瓷上磷酸钙的生长类似。这些支架的生物矿化仅由硅化物相引发,并且可以通过聚合物基质的降解而加速。